Page last updated: 2024-09-03

mk 0663 and Acropachy, Hereditary

mk 0663 has been researched along with Acropachy, Hereditary in 6 studies

Research

Studies (6)

TimeframeStudies, this research(%)All Research%
pre-19900 (0.00)18.7374
1990's0 (0.00)18.2507
2000's0 (0.00)29.6817
2010's4 (66.67)24.3611
2020's2 (33.33)2.80

Authors

AuthorsStudies
Bhagirathi Mallikarjunaswamy, M; Prasad, A; Sehgal, A; Shahi, P1
Li, S; Xu, Y; Yue, H; Zhang, Z1
Fu, WZ; He, JW; Hu, YQ; Li, SS; Liu, YJ; Zhang, ZL1
Guo, L; Sun, F; Ye, S1
Yang, B; Zhang, H1
Li, Z; Wang, D; Wang, S; Yang, Q; Yang, Y1

Trials

1 trial(s) available for mk 0663 and Acropachy, Hereditary

ArticleYear
Clinical, Biochemical, and Genetic Features of 41 Han Chinese Families With Primary Hypertrophic Osteoarthropathy, and Their Therapeutic Response to Etoricoxib: Results From a Six-Month Prospective Clinical Intervention.
    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2017, Volume: 32, Issue:8

    Topics: Adult; Asian People; China; Dinoprostone; Etoricoxib; Family; Female; Humans; Male; Middle Aged; Organic Anion Transporters; Osteoarthropathy, Primary Hypertrophic; Prospective Studies; Pyridines; Sulfones

2017

Other Studies

5 other study(ies) available for mk 0663 and Acropachy, Hereditary

ArticleYear
Incomplete primary hypertrophic osteoarthropathy.
    BMJ case reports, 2020, May-13, Volume: 13, Issue:5

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Combined Modality Therapy; Etoricoxib; Humans; Male; Middle Aged; Osteoarthropathy, Primary Hypertrophic; Physical Therapy Modalities

2020
Monoallelic mutations in SLCO2A1 cause autosomal dominant primary hypertrophic osteoarthropathy.
    Journal of bone and mineral research : the official journal of the American Society for Bone and Mineral Research, 2021, Volume: 36, Issue:8

    Topics: DNA Copy Number Variations; Etoricoxib; Humans; Mutation; Organic Anion Transporters; Osteoarthropathy, Primary Hypertrophic; Pedigree

2021
Primary Hypertrophic Osteoarthropathy With SLCO2A1 Mutation in a Chinese Patient Successfully Treated With Etoricoxib.
    Journal of clinical rheumatology : practical reports on rheumatic & musculoskeletal diseases, 2018, Volume: 24, Issue:3

    Topics: Anti-Inflammatory Agents, Non-Steroidal; Diagnosis, Differential; Etoricoxib; Foot Joints; Hand Joints; Humans; Male; Mutation; Organic Anion Transporters; Osteoarthropathy, Primary Hypertrophic; Tomography, Emission-Computed, Single-Photon; Treatment Outcome; Young Adult

2018
Successful treatment of pachydermoperiostosis patients with etoricoxib, aescin, and arthroscopic synovectomy: Two case reports.
    Medicine, 2017, Volume: 96, Issue:47

    Topics: Arthroscopy; Cardiovascular Agents; Combined Modality Therapy; Cyclooxygenase 2 Inhibitors; Escin; Etoricoxib; Humans; Male; Osteoarthropathy, Primary Hypertrophic; Pyridines; Sulfones; Synovectomy; Treatment Outcome; Young Adult

2017
Successful treatment of pachydermoperiostosis with etoricoxib in a patient with a homozygous splice-site mutation in the SLCO2A1 gene.
    The British journal of dermatology, 2019, Volume: 180, Issue:3

    Topics: Adult; Cyclooxygenase 2 Inhibitors; Dinoprostone; Etoricoxib; Homozygote; Humans; Male; Mutation; Organic Anion Transporters; Osteoarthropathy, Primary Hypertrophic; RNA Splice Sites; Treatment Outcome

2019